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NDC 49483-0716-75 Dual Action Pain Relief 250; 125 mg/1; mg/1 Details

Dual Action Pain Relief 250; 125 mg/1; mg/1

Dual Action Pain Relief is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by TIME CAP LABORATORIES, INC.. The primary component is ACETAMINOPHEN; IBUPROFEN.

MedlinePlus Drug Summary

Acetaminophen is used to relieve mild to moderate pain from headaches, muscle aches, menstrual periods, colds and sore throats, toothaches, backaches, reactions to vaccinations (shots), and to reduce fever. Acetaminophen may also be used to relieve the pain of osteoarthritis (arthritis caused by the breakdown of the lining of the joints). Acetaminophen is in a class of medications called analgesics (pain relievers) and antipyretics (fever reducers). It works by changing the way the body senses pain and by cooling the body.

Related Packages: 49483-0716-75
Last Updated: 04/14/2024
MedLinePlus Full Drug Details: Acetaminophen

Prescription ibuprofen is used to relieve pain, tenderness, swelling, and stiffness caused by osteoarthritis (arthritis caused by a breakdown of the lining of the joints) and rheumatoid arthritis (arthritis caused by swelling of the lining of the joints). It is also used to relieve mild to moderate pain, including menstrual pain (pain that happens before or during a menstrual period). Nonprescription ibuprofen is used to reduce fever and to relieve minor aches and pain from headaches, muscle aches, arthritis, menstrual periods, the common cold, toothaches, and backaches. Ibuprofen is in a class of medications called NSAIDs. It works by stopping the body's production of a substance that causes pain, fever, and inflammation.

Related Packages: 49483-0716-75
Last Updated: 04/14/2024
MedLinePlus Full Drug Details: Ibuprofen

Product Information

NDC	49483-0716
Product ID	49483-716_08acd3bf-ad0d-f693-e063-6394a90ad8c2
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Dual Action Pain Relief
Proprietary Name Suffix	n/a
Non-Proprietary Name	Acetaminophen, Ibuprofen
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	250; 125
Active Ingredient Units	mg/1; mg/1
Substance Name	ACETAMINOPHEN; IBUPROFEN
Labeler Name	TIME CAP LABORATORIES, INC.
Pharmaceutical Class	Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA216994
Listing Certified Through	2024-12-31

Package

NDC 49483-0716-75 (49483071675)

Pricing Information	N/A
NDC Package Code	49483-716-75
Billing NDC	49483071675
Package	1 BOTTLE in 1 CARTON (49483-716-75) / 72 TABLET in 1 BOTTLE
Marketing Start Date	2023-10-13
NDC Exclude Flag	N